Canonical Allele Identifier: CA2610209555
Gene: FFAR4 HGNC NCBI

Linked Data

gnomAD v4: 10-93601793-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601793T>C , CM000672.2:g.93601793T>C GRCh38
NC_000010.10:g.95361550T>C , CM000672.1:g.95361550T>C GRCh37
NC_000010.9:g.95351540T>C NCBI36
NG_009104.1:g.4444A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000604414.1:c.697-2281T>C ENSP00000474477.1:n.697-2281T>C
Search 100 bp 5'
Search 100 bp 3'